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Læknablaðið - 01.05.2016, Blaðsíða 16

Læknablaðið - 01.05.2016, Blaðsíða 16
R A N N S Ó K N 224 LÆKNAblaðið 2016/102 Heimildir 1. Wert S. Normal and abnormal structural development of the lung. In: Polin RA FW, Abam SH, editor. Fetal and neonatal physiology. Saunders, Philadelphia 2004: 783- 801. 2. Clark RH, Gerstmann DR, Jobe AH, Moffitt ST, Slutsky AS, Yoder BA. Lung injury in neonates: causes, strategies for prevention, and long-term consequences. J Pediatr 2001; 139: 478-86. 3. Jobe AH, Bancalari E. Bronchopulmonary dysplasia. Am J Resp Crit Care Med 2001; 163: 1723-9. 4. Baraldi E, Filippone M. Chronic lung disease after premat- ure birth. N Engl J Med 2007; 357: 1946-55. 5. Doyle LW, Ehrenkranz RA, Halliday HL. Late (> 7 days) postnatal corticosteroids for chronic lung disease in pret- erm infants. Cochrane Datab Syst Rev 2014; 5: Cd001145. 6. Postnatal corticosteroids to treat or prevent chronic lung disease in preterm infants. Pediatrics 2002; 109: 330-8. 7. Doyle LW, Ehrenkranz RA, Halliday HL. Early (< 8 days) postnatal corticosteroids for preventing chronic lung dise- ase in preterm infants. Cochrane Datab Syst Rev 2014; 5: Cd001146. 8. Bassler D, Plavka R, Shinwell ES, Hallman M, Jarreau PH, Carnielli V, et al. Early Inhaled Budesonide for the Prevention of Bronchopulmonary Dysplasia. N Engl J Med 2015; 373: 1497-506. 9. Doyle LW, Ehrenkranz RA, Halliday HL. Dexamethasone treatment after the first week of life for bronchop- ulmonary dysplasia in preterm infants: a systematic review. Neonatology 2010; 98: 289-96. 10. Yates HL, Newell SJ. Minidex: very low dose dexa- methasone (0.05 mg/kg/day) in chronic lung disease. Arch Dis Child Fetal Neonatal Ed 2011; 96: F190-4. 11. Cole CH, Colton T, Shah BL, Abbasi S, MacKinnon BL, Demissie S, et al. Early inhaled glucocorticoid therapy to prevent bronchopulmonary dysplasia. N Engl J Med 1999; 340: 1005-10. 12. Jonsson B, Eriksson M, Soder O, Broberger U, Lagercrantz H. Budesonide delivered by dosimetric jet nebulization to preterm very low birthweight infants at high risk for development of chronic lung disease. Acta Paediatrica (Oslo, Norway: 1992) 2000; 89: 1449-55. 13. Jangaard KA, Stinson DA, Allen AC, Vincer MJ. Early prophylactic inhaled beclomethasone in infants less than 1250 g for the prevention of chronic lung disease. Paediatr Child Health 2002; 7: 13-9. 14. Doyle LW, Davis PG, Morley CJ, McPhee A, Carlin JB. Outcome at 2 years of age of infants from the DART study: a multicenter, international, randomized, controlled trial of low-dose dexamethasone. Pediatr 2007; 119: 716-21. 15. Doyle LW, Davis PG, Morley CJ, McPhee A, Carlin JB. Low-dose dexamethasone facilitates extubation among chronically ventilator-dependent infants: a multicenter, international, randomized, controlled trial. Pediatr 2006; 117: 75-83. 16. Jefferies AL, Canadian Paediatric Society F, Newborn C. Postnatal corticosteroids to treat or prevent chronic lung disease in preterm infants. Paediatr Child Health 2012; 17: 573. 17. Walsh MC, Yao Q, Horbar JD, Carpenter JH, Lee SK, Ohlsson A. Changes in the use of postnatal steroids for bronchopulmonary dysplasia in 3 large neonatal networks. Pediatr. 2006; 118: e1328-35. 18. Pantalitschka T, Poets CF. Inhaled drugs for the prevention and treatment of bronchopulmonary dys- plasia. Pediatric Pulmon 2006; 41: 703-8. ENGLISH SUMMARY Introduction: Corticosteroids have been used in preterm infants with immature lungs to decrease their need for supplemental oxygen and mechanical ventilation. Whether the benefits of the treatment outweigh possible adverse effects remains controversial. The main objective of the study was to evaluate the effects of intravenous and inhalation corticosteroids on preterm infants’ need for supplemental oxygen and mechanical ventilation and potential adverse effects. Material and methods: This was a retrospective cohort study on pret- erm infants at the Neonatal Intensive Care Unit of Children’s Hospital Iceland, born between 2000-2014 and treated with intravenous (n=28) or inhalation (n=30) corticosteroids for immature lung disease. For each infant receiving steriods one infant who did not receive steriods was sel- ected as control, matched on gestational age. Results: There was a significant decrease in the need for supplem- ental oxygen following intravenous and inhalation corticosteroids administration, and a significant decrease in the need for mechanical ventilation following intravenous corticosteroids administration, but not in controls. Infants receiving intravenous corticosteroids gained significantly less weight than controls during treatment, but no sign- ificant difference in weight between groups was found at 35 weeks postmenstrual age, or in other possible adverse effects such as the prevalence of cerebral palsy. Conclusion: Intravenous and inhalation corticosteroids decrease the need for supplemental oxygen in preterm infants with immature lung disease and intravenous steriods facilitate earlier weaning from mechanical ventilation, without significant adverse effects. Therefore, it seems justifiable in selected cases to use corticosteroids in treatment of preterm infants with severe immature lung disease. Postnatal corticosteroids in preterm infants with immature lung disease Erna Hinriksdóttir1, Hrólfur Brynjarsson2, Þórður Þórkelsson1,2 1University of Iceland, Faculty of Medicine, 2Children´s Hospital Iceland. Key words: Corticosteroids, preterm infants, chronic lung disease, mechanical ventilation. Correspondence: Þórður Þórkelsson, thordth@landspitali.is Lokaorð Rannsókn þessi leiddi í ljós að gjöf barkstera í æð dregur mark- tækt úr súrefnisþörf fyrirbura með erfiðan lungnasjúkdóm fyrstu dagana eftir að meðferð hefst og minnkar jafnframt þörf þeirra fyrir öndunarvélameðferð, án verulegra aukaverkana. Eina mark- tæka aukaverkunin sem fram kom var tímabundin skerðing á þyngdaraukningu barnanna. Teljum við því að til greina komi, undir sérstökum kringumstæðum, að gefa fyrirburum með erfið- an lungnasjúkdóm barkstera í æð. Leggjum við til að það sé aðeins gert ef sýnt er að ekki takist að ná börnunum af öndunarvél nema gripið sé til þessarar meðferðar. Steragjöf á úðaformi virðist einnig draga úr súrefnisþörf barnanna án merkjanlegra aukaverkana. Því kemur einnig til greina að gefa fyrirburum stera á úðaformi undir vissum kringumstæðum, svo sem til að koma í veg fyrir að börn með vaxandi súrefnisþörf þurfi á öndunarvélameðferð að halda.

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